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Journal Abstract Search

170 related items for PubMed ID: 14510822

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  • 6. Autosomal dominant lateral temporal epilepsy: two families with novel mutations in the LGI1 gene.
    Hedera P, Abou-Khalil B, Crunk AE, Taylor KA, Haines JL, Sutcliffe JS.
    Epilepsia; 2004 Mar; 45(3):218-22. PubMed ID: 15009222
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  • 7. LGI1 microdeletion in autosomal dominant lateral temporal epilepsy.
    Fanciulli M, Santulli L, Errichiello L, Barozzi C, Tomasi L, Rigon L, Cubeddu T, de Falco A, Rampazzo A, Michelucci R, Uzzau S, Striano S, de Falco FA, Striano P, Nobile C.
    Neurology; 2012 Apr 24; 78(17):1299-303. PubMed ID: 22496201
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  • 8. A newly discovered LGI1 mutation in Korean family with autosomal dominant lateral temporal lobe epilepsy.
    Lee MK, Kim SW, Lee JH, Cho YJ, Kim DE, Lee BI, Kim HM, Lee MG, Heo K.
    Seizure; 2014 Jan 24; 23(1):69-73. PubMed ID: 24177143
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  • 10. Screening LGI1 in a cohort of 26 lateral temporal lobe epilepsy patients with auditory aura from Turkey detects a novel de novo mutation.
    Kesim YF, Uzun GA, Yucesan E, Tuncer FN, Ozdemir O, Bebek N, Ozbek U, Iseri SA, Baykan B.
    Epilepsy Res; 2016 Feb 24; 120():73-8. PubMed ID: 26773249
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  • 11. Familial temporal lobe epilepsy with aphasic seizures and linkage to chromosome 10q22-q24.
    Brodtkorb E, Gu W, Nakken KO, Fischer C, Steinlein OK.
    Epilepsia; 2002 Mar 24; 43(3):228-35. PubMed ID: 11906506
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  • 12. Familial temporal lobe epilepsy with psychic auras associated with a novel LGI1 mutation.
    Striano P, Busolin G, Santulli L, Leonardi E, Coppola A, Vitiello L, Rigon L, Michelucci R, Tosatto SC, Striano S, Nobile C.
    Neurology; 2011 Mar 29; 76(13):1173-6. PubMed ID: 21444903
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  • 14. Copy number variations and susceptibility to lateral temporal epilepsy: a study of 21 pedigrees.
    Fanciulli M, Pasini E, Malacrida S, Striano P, Striano S, Michelucci R, Ottman R, Nobile C.
    Epilepsia; 2014 Oct 29; 55(10):1651-8. PubMed ID: 25243798
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  • 15. Mutations in LGI1 gene in Japanese families with autosomal dominant lateral temporal lobe epilepsy: the first report from Asian families.
    Kawamata J, Ikeda A, Fujita Y, Usui K, Shimohama S, Takahashi R.
    Epilepsia; 2010 Apr 29; 51(4):690-3. PubMed ID: 19780791
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  • 16. The clinical phenotype of autosomal dominant lateral temporal lobe epilepsy related to reelin mutations.
    Michelucci R, Pulitano P, Di Bonaventura C, Binelli S, Luisi C, Pasini E, Striano S, Striano P, Coppola G, La Neve A, Giallonardo AT, Mecarelli O, Serioli E, Dazzo E, Fanciulli M, Nobile C.
    Epilepsy Behav; 2017 Mar 29; 68():103-107. PubMed ID: 28142128
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  • 17. Familial mesial temporal lobe epilepsy (FMTLE) : a clinical and genetic study of 15 Italian families.
    Striano P, Gambardella A, Coppola A, Di Bonaventura C, Bovo G, Diani E, Boaretto F, Egeo G, Ciampa C, Labate A, Testoni S, Passarelli D, Manna I, Sferro C, Aguglia U, Caranci F, Giallonardo AT, Striano S, Nobile C, Michelucci R.
    J Neurol; 2008 Jan 29; 255(1):16-23. PubMed ID: 18004642
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  • 18. [Clinical characteristics and LGI1 gene mutation analysis on an autosomal dominant lateral temporal lobe epilepsy].
    Xi ZQ, Wang XF, Lü Y, Wang L, Xiao F, Guan LF.
    Zhonghua Yi Xue Za Zhi; 2009 Jan 20; 89(3):195-7. PubMed ID: 19537038
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  • 19. LGI1 mutations in autosomal dominant and sporadic lateral temporal epilepsy.
    Nobile C, Michelucci R, Andreazza S, Pasini E, Tosatto SC, Striano P.
    Hum Mutat; 2009 Apr 20; 30(4):530-6. PubMed ID: 19191227
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  • 20. Idiopathic partial epilepsy with auditory features (IPEAF): a clinical and genetic study of 53 sporadic cases.
    Bisulli F, Tinuper P, Avoni P, Striano P, Striano S, d'Orsi G, Vignatelli L, Bagattin A, Scudellaro E, Florindo I, Nobile C, Tassinari CA, Baruzzi A, Michelucci R.
    Brain; 2004 Jun 20; 127(Pt 6):1343-52. PubMed ID: 15090473
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